Donate Help Contact The AHA Sign In Home
American Heart Association
Circulation
Search: search_blue_button Advanced Search
Circulation. 2006;113:e771-e773
doi: 10.1161/CIRCULATIONAHA.105.594200
This Article
Right arrow Full Text (PDF)
Right arrow Data Supplement
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrow Request Permissions
Citing Articles
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Tadamura, E.
Right arrow Articles by Togashi, K.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Tadamura, E.
Right arrow Articles by Togashi, K.
Related Collections
Right arrow Other Treatment
Right arrow CT and MRI
Right arrow Nuclear cardiology and PET
Right arrowRelated Article

(Circulation. 2006;113:e771-e773.)
© 2006 American Heart Association, Inc.


Images in Cardiovascular Medicine

Multimodality Imaging of Cardiac Sarcoidosis Before and After Steroid Therapy

Eiji Tadamura, MD, PhD; Masaki Yamamuro, MD; Shigeto Kubo, MD, PhD; Shotaro Kanao, MD; Ryohei Hosokawa, MD, PhD; Takeshi Kimura, MD, PhD; Toru Kita, MD, PhD; Kaori Togashi, MD, PhD

From the Department of Diagnostic Imaging and Nuclear Medicine, Kyoto University Graduate School of Medicine, Kyoto, Japan (E.T., M.Y., S. Kubo, S. Kanao, K.T.); and the Department of Cardiovascular Medicine, Kyoto University Graduate School of Medicine, Kyoto, Japan (R.H., T. Kimura, T. Kita).

Correspondence to Eiji Tadamura, MD, Department of Diagnostic Imaging and Nuclear Medicine, Kyoto University Graduate School of Medicine, 54 Shogoinkawahara, Sakyo-ku, Kyoto, 606-8507, Japan. E-mail et{at}kuhp.kyoto-u.ac.jp

A 65-year-old woman was referred to our hospital because of chest pain. Right ventricular bundle-block was noted on the ECG. Angiotensin-converting enzyme level was elevated (33.2 IU/L). Delayed-enhanced magnetic resonance imaging (MRI) using an inversion-recovery segmented gradient echo sequence performed 15 minutes after gadolinium contrast injection (0.15 mmol/kg of gadodiamide) disclosed hyperenhancement, mainly in the outer layer of the septal, inferior, and anterolateral walls (Figure 1A). Cine MRI revealed wall motion abnormalities in septal and inferior walls (Figure 1B and 1C; Movie I). Left ventricular ejection fraction was 44%. Resting 201thallium single photon emission tomography revealed perfusion defects in these walls (Figure 1D). Positron emission tomography with 18fluorodeoxyglucose (FDG PET) imaging performed in a fasting condition showed FDG accumulation in the septal, inferior, and anterolateral walls, corresponding to areas with late enhancement (Figure 1E). Whole-body FDG PET imaging depicted significant FDG uptake not only in the heart but also in the hilar, mediastinal, and cervical lymph nodes (Figure 2, Movie II, left). Cardiac involvement of sarcoidosis was confirmed by histological analysis of endomyocardial biopsy. After 6 months of steroid therapy, her angiotensin-converting enzyme level was decreased (13.1 IU/L). Areas with delayed enhancement were markedly diminished (Figure 3A). Wall motion abnormalities (Figure 3B and 3C; Movie III) and perfusion abnormalities (Figure 3D) in the septal and inferior walls were not significantly changed. Her left ventricular ejection fraction was 41%. FDG accumulation was surprisingly decreased in the heart and lymph nodes (Figure 4, Movie II, right).


Figure 1175299
View larger version (71K):
[in this window]
[in a new window]
 
Figure 1. A short-axis image of delayed-enhanced MRI reveals severe extent of hyperenhancement in septal, inferior, and anterolateral regions (white arrows). B and C, Cine MRI obtained at end diastole (B) and end systole (C) in a basal short-axis slice show wall motion abnormalities in septal and inferior walls (black arrows). Also see Movie I. D, A short-axis image of 201thallium single photon emission tomography demonstrates perfusion defects in septal and inferior regions (white arrows), where severe extent of enhancement is seen in a delayed enhanced MR image. E, A short-axis image of fasting FDG PET shows FDG accumulation in septal, inferior, and anterolateral walls (white arrows), corresponding to areas with late enhancement.


Figure 2175299
View larger version (83K):
[in this window]
[in a new window]
 
Figure 2. Whole-body FDG PET image in a fasting condition shows striking FDG accumulation in the hilar, mediastinal, and cervical lymph nodes and the heart. Also see Movie II, left.


Figure 3175299
View larger version (60K):
[in this window]
[in a new window]
 
Figure 3. A, Areas of hyperenhancement in the septal, inferior, and anterolateral regions are considerably decreased after steroid therapy (white arrows). B and C, Cine MRI obtained at end diastole (B) and end systole (C) in a short-axis slice show wall motion abnormalities even after steroid therapy (black arrows). Also see Move III. D, 201Thallium perfusion defects in septal and inferior walls (white arrows) are not significantly improved after steroid therapy.


Figure 4175299
View larger version (61K):
[in this window]
[in a new window]
 
Figure 4. Whole-body FDG PET image in a fasting condition shows the marked reduction of FDG uptake in the heart and lymph nodes after steroid therapy. Also see Movie II, right.

Before steroid therapy, areas with hyperenhancement in the delayed-enhanced images corresponded to the areas with decreased 201thallium defects, increased FDG uptake, and wall motion abnormalities. Thus, delayed enhancement in contrast-enhanced MRI is considered to reflect fibrogranulomatous tissues of sarcoidosis replacing the normal myocardium. The number of areas with late enhancement and FDG uptake in the heart was surprisingly decreased after the suppression of the disease activities by the steroid therapy, whereas wall motion abnormalities were not significantly improved. The pathophysiological condition of cardiac sarcoidosis has been clearly identified by multimodality imaging.


*    Footnotes
 
The online-only Data Supplement, which contains 3 movies, is available at http://circ.ahajournals.org/cgi/content/full/113/20/e771/DC1.


Related Article:

Issue Highlights
Circulation 2006 113: 2373. [Full Text]




This Article
Right arrow Full Text (PDF)
Right arrow Data Supplement
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrow Request Permissions
Citing Articles
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Tadamura, E.
Right arrow Articles by Togashi, K.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Tadamura, E.
Right arrow Articles by Togashi, K.
Related Collections
Right arrow Other Treatment
Right arrow CT and MRI
Right arrow Nuclear cardiology and PET
Right arrowRelated Article